跳至主要内容
临床试验/NL-OMON39302
NL-OMON39302已完成2 期

Memantine Add-On Therapy to Clozapine - MAOTC

GGZ NH0 个研究点目标入组 52 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
52

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Eligible for the study are outpatients, both sexes, age 18 to 60, meeting DSM-IV criteria for schizophrenia, based on the definitions in the Mini International Neuropsychiatric Interview Plus (MINI-Plus) with persistent residual psychopathology, failing to achieve the remission criteria, after adequate treatment with clozapine for at least 6 months. Before the start of the study clozapine plasma concentration has been at least 350 ng/ml for 12 weeks or has not reached 350 ng/ml due to intolerability. Remission defined as simultaneous ratings of mild or less (<= 3 points) on 8 of the PANSS items evaluating the core symptoms of schizophrenia (P1 delusions, G9 unusual thought content, P3 hallucinatory behaviour, P2 conceptual disorganisation, G5 mannerisms and posturing, N1 blunted affect, N4 passive or apathetic social withdrawal, N6 lack of spontaneity and flow of conversation) (Os van and Kahn, 2007). Patients should be able to understand the study information and procedures and give informed consent. All participants fulfilling the inclusion and not fulfilling the exclusion criteria may, after a detailed description by a doctor and the written declaration of informed consent on an according form, participate in the study.

排除标准

  • - Pregnancy.
  • - Lactating women.
  • - Female subjects without adequate contraception.
  • - Known hypersensitivity to memantine or ingredients used in this tablet.
  • - Uncontrolled epilepsy.
  • - Recent myocardial infarction.
  • - Uncontrolled hypertension.
  • - Renal insufficiency (GFR less than 30 ml/min).
  • - Severe liver failure (ASAT 175 U/l and/or ALAT 225 U/l in men and 175 U/l in women).
  • - Lactose intolerance.
  • - Co-medication with NMDA-antagonists such as amantadine, ketamine, dextromethorphan.
  • -Co-medication with glutamate antagonists such as lamotrigine and topiramate.
  • - Extremely ill patients (Global Assessment of Functioning [GAF] <= 20), who are not reliably able to give their informed consent.
  • - Moderate or severe Alzheimer*s disease.

研究者

发起方
GGZ NH

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